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Session 5 Track 4: IDMP Implementation - Where is the Correct Data?
Session Chair(s)
Hans van Bruggen, MSC
Director of Regulatory Affairs
Celegence, United States
Learning Objective : Participants will be able to - recognise advantages and disadvantages of the ‘Single Place of Truth’ - evaluate the different approaches to medicinal product life cycle - explain the concept of information reuse in RIM
Speaker(s)
Data’s Revenge or Why RIM’s Emerging Dossier Concept Should be Served from a ‘Single Place of Truth’
Olaf Schoepke, PHD
Samarind, United Kingdom
Vice President, Regulatory Solutions
Developing RIM Solution to Access Accurate, Streamlined and Real Time Regulatory Information for Pharma/Biopharma Companies
Abhishek Harde, MBA, MPHARM, RAC
United States
Source Data: The Future of Regulatory Affairs
Hans van Bruggen, MSC
Celegence, United States
Director of Regulatory Affairs